日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Parental origin of deletions and duplications - about the necessity to check for cryptic inversions

缺失和重复的亲本来源——关于检查隐性倒位的必要性

Liehr, Thomas; Schreyer, Isolde; Kuechler, Alma; Manolakos, Emmanouil; Singer, Sylke; Dufke, Andreas; Wilhelm, Kathleen; Jančušková, Tereza; Čmejla, Radek; Othman, Moneeb A K; Al-Rikabi, Ahmed H; Mrasek, Kristin; Ziegler, Monika; Kankel, Stefanie; Kreskowski, Katharina; Weise, Anja

A Girl with 10 Mb Distal Xp Deletion Arising from Maternal Pericentric Inversion: Clinical Data and Molecular Characterization

一名患有10 Mb远端Xp缺失的女孩,其病因是母系近着丝粒倒位:临床数据和分子特征

Papoulidis, Ioannis; Vetro, Annalisa; Paspaliaris, Vassilis; Ziegler, Monika; Kreskowski, Katharina; Daskalakis, George; Papadopoulos, Vasilios; Dagklis, Themistoklis; Liehr, Thomas; Thomaidis, Loretta; Manolakos, Emmanouil

X-autosome and X-Y Translocations in Female Carriers: X-chromosome Inactivation Easily Detectable by 5-ethynyl-2-deoxyuridine (EdU)

女性携带者中的 X-常染色体和 XY 易位:5-乙炔基-2-脱氧尿苷 (EdU) 可轻松检测 X 染色体失活

Donat, M; Louis, A; Kreskowski, K; Ziegler, M; Weise, A; Schreyer, I; Liehr, T

Heteromorphic variants of chromosome 9

9号染色体的异型变异

Kosyakova, Nadezda; Grigorian, Ani; Liehr, Thomas; Manvelyan, Marina; Simonyan, Isabella; Mkrtchyan, Hasmik; Aroutiounian, Rouben; Polityko, Anna D; Kulpanovich, Anna I; Egorova, Tatiana; Jaroshevich, Evgenia; Frolova, Alla; Shorokh, Natalia; Naumchik, Irina V; Volleth, Marianne; Schreyer, Isolde; Nelle, Heike; Stumm, Markus; Wegner, Rolf-Dieter; Reising-Ackermann, Gisela; Merkas, Martina; Brecevic, Lukretija; Martin, Thomas; Rodríguez, Laura; Bhatt, Samarth; Ziegler, Monika; Kreskowski, Katharina; Weise, Anja; Sazci, Ali; Vorsanova, Svetlana; Cioffi, Marcelo de Bello; Ergul, Emel

Complex small supernumerary marker chromosomes - an update

复杂小型超数标记染色体——最新进展

Liehr, Thomas; Cirkovic, Sanja; Lalic, Tanja; Guc-Scekic, Marija; de Almeida, Cynthia; Weimer, Jörg; Iourov, Ivan; Melaragno, Maria Isabel; Guilherme, Roberta S; Stefanou, Eunice-Georgia G; Aktas, Dilek; Kreskowski, Katharina; Klein, Elisabeth; Ziegler, Monika; Kosyakova, Nadezda; Volleth, Marianne; Hamid, Ahmed B

Molecular Cytogenetic Study of the NF2 Gene Deletion in Meningioma in Sudanese Patients

苏丹患者脑膜瘤中NF2基因缺失的分子细胞遗传学研究

Abdelmontalab, Farah Y; Fadl, Elmula I; Abushama, Hm; Kreskowski, K; Liehr, T

Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangements

携带体质平衡染色体重排的个体中脆性位点与染色体断裂点相关性的证据

Liehr, T; Kosayakova, N; Schröder, J; Ziegler, M; Kreskowski, K; Pohle, B; Bhatt, S; Theuss, L; Wilhelm, K; Weise, A; Mrasek, K

Noel Frank Collett Gowing

诺埃尔·弗兰克·科莱特·戈温

Manvelyan, Marina; Cremer, Friedrich W; Lancé, Jeannette; Kläs, Rüdiger; Kelbova, Christina; Ramel, Christian; Reichenbach, Herbert; Schmidt, Catharina; Ewers, Elisabeth; Kreskowski, Katharina; Ziegler, Monika; Kosyakova, Nadezda; Liehr, Thomas; Kane, Stephen; Cilia-Vincenti, Albert